QA SPECIALIST MEDICAL DEVICES jobs in UNITED KINGDOM, United Kingdom

Regulatory Affairs Specialist - Medical Devices company-West Yorkshire - £negotiable, pension, 23 days holiday + BHs... successful medical devices company at their West Yorkshire based head office. The Company They are a market leading, medical devices...

Vitalograph is a leading manufacturer of medical respiratory diagnostic devices and software, used in the diagnosis.... We are now recruiting for a QA Specialist to join our growing team in Buckingham. With celebrating 60 years in business, expansion plans...

. Ideal Requirements for a Quality Assurance and Regulatory Affairs Manager Experience working with medical devices either in... or allowance, pension and more! Innovative Product Portfolio: Work with a leading Ophthalmic product range in a specialist market...

: We are looking to recruit a full-time and permanent QA Specialist to work within the quality assurance team based in Manchester. The QA... of ISO13485, ISO15189 or ISO9001 requirements Previous experience working with In Vitro Devices (IVD/IVDR) or Medical Devices...

Job title: Clinical Affairs Specialist Reports to: Global Head of QA/RA Location: Manchester Science Park / Hybrid...-vitro diagnostic medical devices, ensuring compliance with the ISO 20916:2019 standard and IVDR requirements. Ensure...

innovative medical devices, which we use in clinical trials to collect a biobank of mucus-based biospecimens. This biobank... System (QMS). With understanding of ISO: 13485. This Role is more QA but knowledge of RA beneficial. Support the...

of life. Whether it’s next-generation diagnostics, life-changing devices, science-based nutrition, or novel reformulations.... This role is responsible to ensure all Worldwide Supplier QA activities for high rated suppliers, including customer...

setting (preferred) Knowledge of global regulatory requirements for pharmaceutical, medical devices and combination products... role The Reporting Specialist is responsible for executing all of the reporting, in partnership with internal...

industry or in a clinical setting (preferred) Knowledge of global regulatory requirements for pharmaceutical, medical devices... to join their team in Marlow. Purpose of the role The Reporting Specialist is responsible for executing all of the reporting, in...

Team. You will act as the Medical Physics Expert for the facility and will be responsible for actioning and overseeing.... You will also work closely with PETIC's Radioactive Waste Advisor and Dangerous Goods Safety Advisors as well as the Medical Physicists...

validation (e.g. GAMP5 or IPSE) Practical experience in QA and/or Validation roles within the Pharmaceutical and/or Medical... Validation Engineer needs to provide Validation leadership, Specialist Knowledge and Executes validation projects, ensuring these...